510(k) K894689 ยท CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
PENLON IDP PRESSURE FAILURE ALARM
| Applicant | Penlon, Inc., Riverside CA, US |
| Decision | Substantially Equivalent, Aug 10, 1989 |
| Received | Jul 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894689
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.